NM_001159699.2(FHL1):c.856C>G (p.Gln286Glu) AND Cardiovascular phenotype
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 7, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004026190.1
Allele description [Variation Report for NM_001159699.2(FHL1):c.856C>G (p.Gln286Glu)]
NM_001159699.2(FHL1):c.856C>G (p.Gln286Glu)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Sep 29, 2024